CASE OF (13Q-18Q) TRANSLOCATION WITH PROXIMAL 13Q MONOSOMY

被引:6
作者
SUZUKI, Y
ONO, K
OKA, S
MATSUBARA, T
ARIMA, M
NAKAGOME, Y
机构
[1] TOTTORI UNIV,SCH MED,INST NEUROL SCI,DIV CHILD NEUROL,YONAGO,TOTTORI 683,JAPAN
[2] NATL INST GENET,DEPT HUMAN GENET,MISHIMA,SHIZUOKA 411,JAPAN
关键词
D O I
10.1007/BF00402161
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:337 / 341
页数:5
相关论文
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  • [2] GROUCHY JD, 1969, BIRTH DEFECTS OAS, V5, P74
  • [3] NOEL B, 1976, CLIN GENET, V9, P593
  • [4] SCHWANITZ G, 1975, HUMANGENETIK, V28, P93, DOI 10.1007/BF00735740
  • [5] CLINICAL AND CHROMOSOMAL STUDIES OF 18Q- SYNDROME
    WERTELECKI, W
    GERALD, PS
    [J]. JOURNAL OF PEDIATRICS, 1971, 78 (01) : 44 - +